CH145327A - Process for the preparation of an azophthalein dye. - Google Patents
Process for the preparation of an azophthalein dye.Info
- Publication number
- CH145327A CH145327A CH145327DA CH145327A CH 145327 A CH145327 A CH 145327A CH 145327D A CH145327D A CH 145327DA CH 145327 A CH145327 A CH 145327A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- azophthalein
- acid
- red
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Azophtaleinfarbstoffes. Gegenstand dieser Erfindung ist ein Ver fahren zur Darstellung eines Azophtalein- farbstoffes von nachstehender Formel:
EMI0001.0005
welches dadurch gekennzeichnet ist, dass man den Monoazofarbstoff aus Anthranilsäure und Resorcin mit Dimethylamido-m-oxyben- zoylbenzoesäure im Verhältnis gleicher Mole küle kondensiert.
<I>Beispiel:</I> 26 Teile des Farbstoffes aus Anthranil- säure und Resorcin werden mit 28,5 Teilen Dimethylamido - m - ogybenzoylbenzoesäure vermischt und eingetragen in 300 Teile kon- zentrierte Schwefelsäure. Man rührt 24 Stunden bei<B>80',</B> giesst in Wasser und fil- triert die vollständig ausgeschiedene Farb- stoffsäure ab. Sie bildet getrocknet ein dunkles Pulver, das sich in Wasser auf Zu satz von Alkalien rot, in konzentrierter Schwefelsäure braun löst.
Die nachchromier- ten Färbungen auf Wolle und Seide des nach bekannten Verfahren in das Alkalisalz über geführten Farbstoffes sind braunrot.
Process for the preparation of an azophthalein dye. The subject of this invention is a process for the preparation of an azophtalein dye of the following formula:
EMI0001.0005
which is characterized in that the monoazo dye from anthranilic acid and resorcinol is condensed with dimethylamido-m-oxybenzoylbenzoic acid in proportions of the same molecules.
<I> Example: </I> 26 parts of the dye made from anthranilic acid and resorcinol are mixed with 28.5 parts of dimethylamido - m - ogybenzoylbenzoic acid and added to 300 parts of concentrated sulfuric acid. The mixture is stirred for 24 hours at <B> 80 ', </B> poured into water and the completely separated dye acid is filtered off. When dried, it forms a dark powder that dissolves red in water with the addition of alkalis and brown in concentrated sulfuric acid.
The re-chromed dyeings on wool and silk of the dye converted into the alkali salt by known processes are brown-red.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE145327X | 1928-05-24 | ||
CH142447T | 1929-05-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH145327A true CH145327A (en) | 1931-02-15 |
Family
ID=25714076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH145327D CH145327A (en) | 1928-05-24 | 1929-05-21 | Process for the preparation of an azophthalein dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH145327A (en) |
-
1929
- 1929-05-21 CH CH145327D patent/CH145327A/en unknown
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